What is sexual reproduction and its origin? Sexual reproduction: Sexual reproduction is a type of reproduction that involves a complete life cylce in which a gamete with a single set of chromosomes combine with another to produce an organisms composed of cell with two set of chromosomes. Explanation: In the production of sex cell in eukaryotes diploid mother cell divide to produce haploid cell known as gametes in a process called meiosis.The homologus chromosomes pair up so that their DNA sequence are aligned with each other so this is followed by the exchange of genetic information between them. Two rounds of cell division then produce 4 haploid gametes each with half number of chromosomes from each parent cell,but with the genetic information in the parental chromosomes recombined.Two haploid gametes combine into a one diploid cell known as a zygote in a process called fertilization. In human reproduction each cell contain 46 chromosomes in 23 pairs.Meiosis in parent gonads produces gametes that each contain only 23 chromosomes.When the nuclei of the gametes come close togather to form a fertilized egg each cell of the resulting child will have 23 chromosomes. Sexual reproduction in different animals: INSECTS: Insect species reproduce sexually. Typically they have two sexes with male producing spermatozoa and female ova.Ova develop into a egg that have a covering called the chorion which forms before internal fertilization . BIRDS: Birds have two sexes: either female or male. The sex of birds is determined by the Z and W sex chromosomes, rather than by the X and Y chromosomes present in mammals. Male birds have two Z chromosomes (ZZ), and female birds have a W chromosome and a Z chromosome Mammals: Most mammals are viviparous, giving birth to live young. However, the five species of monotreme, the platypuses and the echidnas, lay eggs. The monotremes have a sex determination system different from that of most other mammals. Origin of sexual reproduction: Sex Evolves When Selection Changes Over Time: Current models indicate that sex evolves more readily when a species' environment changes rapidly. When the genetic associations built up by past selection are no longer favorable, sex and recombination can improve the fitness of offspring, thereby turning the recombination load into an advantage. One important source of environmental change is a shift in the community of interacting species, especially host and parasite species. This is the so-called "Red Queen" hypothesis for the evolution of sex, which refers to the need for a species to evolve as fast as it can just to keep apace of coevolving species Increased allocation to sexual reproduction can evolve because of "Red Queen" interactions, but only if selection is strong enough to cause rapid switches in which gene combinations are favorable. Sex Evolves When Selection Changes Over Space: Sex can also be favored when selection varies over space, as long as the genetic associations created by migration are locally disadvantageous. Whether this requirement is common in nature remains an open question. Sex Evolves When Organisms Are Less Adapted to Their Environment: Organisms that reproduce both sexually and asexually tend to switch to sex under stressful conditions. Mathematical models have revealed that it is much easier for sex to evolve if individuals that are adapted to their environment reproduce asexually and less fit individuals reproduce sexually. In this way, well-adapted genotypes are not broken apart by recombination, but poorly adapted genotypes can be recombined to create new combinations in offspring. Sex Evolves When Populations Are Finite: Models that account for the fact that population sizes are finite have found that sex and recombination evolve much more readily. With a limited number of individuals in a population, selection erodes easily accessible variation, leaving only hidden variation .
Recombination can then reveal this hidden variation,
improving the response to selection. By improving the response to selection, genes that increase the frequency of sex become associated with fitter genotypes, which rise in frequency alongside them. Interestingly, the requirement that fitness surfaces exhibit weak and negative curvature is relaxed in populations of finite size; here, fitness surfaces may be uncurved or positively curved and still favor sex.